| Tag | Content |
|---|
EnhancerAtlas ID | HS138-44205 | Organism | Homo sapiens | Tissue/cell | MSC_BM | Coordinate | chr9:131066020-131067880 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr9:131067663-131067675 | GTTTGTTTGTTT | + | 6.32 | | KLF14 | MA0740.1 | chr9:131067565-131067579 | GGCCACGCCCCTCC | + | 6.25 | | SP3 | MA0746.2 | chr9:131067565-131067578 | GGCCACGCCCCTC | + | 6.18 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGGGAAGAGC TGGTCTTGGG GAAAGATGAC GAGTTAGGAT TCAGAAGTGT TCAGTTTGAG 60
ATGCAAACAC AGCTCCTAAG TGGAAATGCT TAACGGTATA ATGGAGTTCA TGGGAGAAGT 120
CAGGCTAAAG GTGTAAAAAT GGGCACCATC AGTATAATGC TATTAAAAAC CATGGTGGCC 180
AGGTGCAGTG GCTCATGCCT GTAATCCCAC TACTTTGGGA GGCTGAGGTG AGCAGTTCAC 240
CTGAGTCTAG GATTTGAGAC TAGCCTGGGC AACATGGCAA AACCCTGTCT CTACAAAAAA 300
TACAAAAATT AGCCAGGCAT GGTGGCTCAT ACCTGTAGTC CCAGCTCCTC GGGAGGCTGA 360
GGCATGAGAA TCACTTCAAC CCAGGAGGTG GAGGTTGCAG TGAGCTGAGA TCACGCCACT 420
ACACAACAAA AGAGCGAGAC TGGGCAACAG GGCGAGACTC TATCTCAAAA CAACAATAAG 480
AAAAACCATG GCAATATTGA GTTGATGTCA CCAAGGGACT GGGTGTGGGC AGAGGAAGAA 540
CCAGGACCAG AGGAGAGCTC AGGAGAGGAG GAGCCCCACA AAGGAGACTG AGAAGGAACC 600
AGGGAGGGAG ACGGGGAGAC CAGGAGGAGC CTCCTGAAGG CAATGTTTTT TGGGAGGAGG 660
CAGTGACCAG CTGTGTGAGA TGCTGCTGAG AAGGAGCTGC TGGATTTAAC CAGGAGGAGG 720
TCATTGTTGA CCTTGACAAG TCATTTCAGG AGCGTTTTGG CGAAGGAGAG TCTGACTGGC 780
ATGGATTCAG GGCAGTGTGG GAAGAGAGGA ACTGGGGACA GTGACTACAG ACAACCTTTC 840
CAGGAGTTTT GCTCTAAAGG AGGCAAAGGA ATGCAGTAAT TGTAGAGTTA TGAGGTCAAG 900
AAAGAGCTTT TGTTTTGTTT TTATGGTTTT TATGTGGGTG TGATAAAATG TGCATAATGT 960
AAAATTTATC ATTTTAGCCT TTTTTTTTTA AGAGTTGAGG GTCTTAATTA GCCAGGTGTC 1020
ACGGTGTGCA TCTGTAGTCT CAGCTACTTG GGAGGCTGAG GTGGGAGAAT CACTTGAGCC 1080
TGGGAGGCAG AGGTTGCAGT GAGCTAAGAT TGCGCCACTA CACTCCAGCC TAGGTGACAA 1140
AGTGAGACTC TGTCTCAAAA AAAAAAAAAA ATTACGTACA TACTTATATA TAAAATGAAT 1200
CAGCTCCCAA GCCTCTGCTT CACTGACCAG CCAGATCTCC TCCCTGTGCT CATCACTCCA 1260
TTATTTTCTT GCCTGATCCC CCTACGTCAT AATCTCTGTG AGACCTAGAG CCTCATCTGT 1320
CCTTGAGTAC CAAGTCCCAG CACCCAGAGC AGTGGCTGGC CTACAGGAGC ACGCGATTAA 1380
CACACGTGGG TGGGATGAAA GACAATGAGC AAGTGAGTGT CGTTTTAATC CCCATTTTAT 1440
AGATAGGTGA CAGCTTCAGA GGCCACATTA CCCAGTCAGT AAACACAGTA AGCTGAGGTT 1500
CCACCCAGGC CCTTTGGCTG TGAAAGCCAA GATGAGTAGC CTGGGGGCCA CGCCCCTCCC 1560
CCAGGTGCCC AGTTCATACA GGCAGGCAAT TGGCAGACGT GGGGGCCTGT GGATTTGTCA 1620
GCAAGGTTGC TGGTGGGGTT TTTGTTTGTT TGTTTTGAGA TAGGGTCTCA CCCTGTCACC 1680
CAGGCTAGAG TACAGTCGTG TGATTTCAGC TCACTGCAAC CTCCACCTCC TGGGTTCAAA 1740
TGATTCTCCC ACCTCAGCCC AGATCTGGAG TAGCTGTAGC TGGACTACAG ACAAGCGCCA 1800
CCATGCCCGG CTAATTTTTG TATTTTTGGT AGAGACAGGG TTTCACCATA TTGGCCAGGC 1860
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